Gail Coghlan

A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia

Lionel Arnaud, Carole Saison, Virginie Helias et al. · The American Journal of Human Genetics · 2010 · 196 citations · Full text

Transcriptional Regulation, Developmental Biology, Genetic Disorder +10

Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome

Joy Armistead, Sunita Khatkar, Britta Meyer et al. · The American Journal of Human Genetics · 2009 · 124 citations · Full text

Genome Instability, Ribosome Biogenesis, Mendelian Disorder +8

GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

Dan Doherty, Albert E. Chudley, Gail Coghlan et al. · The American Journal of Human Genetics · 2012 · 122 citations · Full text

Mendelian Disorder, Brain Malformations, Genetic Disorder +7

A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus

Tracey Weiler, Cheryl R. Greenberg, Teresa Zelinski et al. · The American Journal of Human Genetics · 1998 · 114 citations · Full text

Genetic Analysis, Developmental Biology, Mendelian Disorder +7

Helicobacter Pylori in The Canadian Arctic: Seroprevalence and Detection in Community Water Samples

Iris McKeown, Pamela Orr, Sharon Macdonald et al. · The American Journal of Gastroenterology · 1999 · 91 citations